MRPL4[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2235392	NM_015956.3(MRPL4):c.119G>A (p.Ser40Asn)	MRPL4 (S40N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232545	NM_015956.3(MRPL4):c.401G>C (p.Gly134Ala)	MRPL4 (G134A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407443	NM_015956.3(MRPL4):c.509G>A (p.Arg170Gln)	MRPL4 (R170Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3207782	NM_015956.3(MRPL4):c.592G>A (p.Gly198Arg)	MRPL4 (G198R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 403106	NM_015956.3(MRPL4):c.740-13A>C	MRPL4	Single nucleotide variant (3 prime UTR variant +1 more)	not specified +1 more	GBenign
Select item 403107	NM_015956.3(MRPL4):c.740-8G>C	MRPL4	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GBenign

ClinVar